Regulation and functional role of eEF1A2 in pancreatic carcinoma

被引:40
作者
Cao, Haixia [1 ]
Zhu, Qi [1 ]
Huang, Jia [1 ]
Li, Baiwen [1 ]
Zhang, Su [1 ]
Yao, Weiyan [1 ]
Zhang, Yongping [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Rui Jin Hosp, Dept Gastroenterol, Shanghai 200025, Peoples R China
关键词
eEF1A2; Protein translation; Pancreatic cancer; Cell growth and invasion; ELONGATION-FACTOR EEF1A2; PROTEIN-SYNTHESIS; FACTOR; 1-ALPHA; EXPRESSION; TRANSLATION; ACTIN; CELLS; ISOFORM; GROWTH; CANCER;
D O I
10.1016/j.bbrc.2008.12.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic cancer typically has all unfavourable prognosis due to late diagnosis and a lack of therapeutic options. Thus, it is important to better understand its pathological mechanism and to develop more effective treatments for the disease. Human chromosome 20q13 has long been suspected to harbour oncogenes involved in pancreatic cancer and other tumours. In this Study, we found that eEF1A2, a gene located in 20q13, was significantly upregulated in pancreatic cancer. Little or no expression of eEF1A2 was detected in normal human pancreatic and chronic pancreatitis tissues, whereas increased eEF1A2 expression occurred in 83% of the pancreatic cancers we studied, Furthermore, using in vitro and in vivo model systems, we found that overexpression of eEF1A2 promoted cell growth, survival, and invasion in pancreatic cancer. Our data thus suggest that eEF1A2 might play an important role in pancreatic carcinogenesis, possibly by acting as a tumour oncogene. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:11 / 16
页数:6
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